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15128-90-2

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15128-90-2 Usage

Description

3-Hydroxy-6-methyl-2-nitropyridine is a yellow fine crystalline powder with a unique molecular structure that has been investigated using density functional theory (DFT). It is an organic compound with the molecular formula C6H6N2O3, featuring a pyridine ring with a hydroxyl group at the 3-position, a methyl group at the 6-position, and a nitro group at the 2-position.

Uses

Used in Chemical Synthesis:
3-Hydroxy-6-methyl-2-nitropyridine is used as an intermediate in the synthesis of various organic compounds, including 3-methoxy-6-methyl-2-nitropyridine. Its unique structure makes it a valuable building block for the development of new molecules with potential applications in various fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-hydroxy-6-methyl-2-nitropyridine is used as a starting material for the development of new drugs. Its molecular structure and properties make it a promising candidate for the synthesis of novel therapeutic agents, particularly in the areas of medicinal chemistry and drug design.
Used in Material Science:
3-Hydroxy-6-methyl-2-nitropyridine's unique chemical properties also make it a candidate for use in the development of new materials, such as polymers and coatings, with specific properties tailored for various applications in the material science industry.
Used in Analytical Chemistry:
The molecular structure and vibrational assignments of 3-hydroxy-6-methyl-2-nitropyridine have been investigated using density functional theory (DFT), making it a subject of interest in analytical chemistry. 3-HYDROXY-6-METHYL-2-NITROPYRIDINE can be used as a reference material for the development and validation of new analytical techniques and methods in the field.

Check Digit Verification of cas no

The CAS Registry Mumber 15128-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,2 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15128-90:
(7*1)+(6*5)+(5*1)+(4*2)+(3*8)+(2*9)+(1*0)=92
92 % 10 = 2
So 15128-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O3/c1-4-2-3-5(9)6(7-4)8(10)11/h2-3,9H,1H3

15128-90-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L07074)  3-Hydroxy-6-methyl-2-nitropyridine, 99%   

  • 15128-90-2

  • 10g

  • 468.0CNY

  • Detail
  • Alfa Aesar

  • (L07074)  3-Hydroxy-6-methyl-2-nitropyridine, 99%   

  • 15128-90-2

  • 50g

  • 1402.0CNY

  • Detail
  • Aldrich

  • (232742)  3-Hydroxy-6-methyl-2-nitropyridine  99%

  • 15128-90-2

  • 232742-10G

  • 449.28CNY

  • Detail
  • Aldrich

  • (232742)  3-Hydroxy-6-methyl-2-nitropyridine  99%

  • 15128-90-2

  • 232742-50G

  • 1,341.99CNY

  • Detail

15128-90-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Hydroxy-6-methyl-2-nitropyridine

1.2 Other means of identification

Product number -
Other names 3-Hydroxy-6-Methyl-2-nitropyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15128-90-2 SDS

15128-90-2Relevant articles and documents

Iodine(III)-Catalyzed Electrophilic Nitration of Phenols via Non-Br?nsted Acidic NO2+ Generation

Juárez-Ornelas, Kevin A.,Jiménez-Halla, J. Oscar C.,Kato, Terumasa,Solorio-Alvarado, César R.,Maruoka, Keiji

supporting information, p. 1315 - 1319 (2019/03/07)

The first catalytic procedure for the electrophilic nitration of phenols was developed using iodosylbenzene as an organocatalyst based on iodine(III) and aluminum nitrate as a nitro group source. This atom-economic protocol occurs under mild, non-Br?nsted acidic and open-flask reaction conditions with a broad functional-group tolerance including several heterocycles. Density functional theory (DFT) calculations at the (SMD:MeCN)Mo8-HX/(LANLo8+f,6-311+G) level indicated that the reaction proceeds through a cationic pathway that efficiently generates the NO2+ ion, which is the nitrating species under neutral conditions.

3-Pyridyl enantiomers and their use as analgesics

-

, (2008/06/13)

The present invention relates to a method of controlling pain in mammals, including humans, comprising administering to a mammal or patient in need of treatment thereof selected compounds of formula I: STR1 or a pharmaceutically acceptable salt thereof. The invention further relates to selected (R) and (S) compounds of formula I above which are useful as analgesics as well as neuronal cell death preventors and anti-inflammatories.

Medicinal oxazolopyridine compounds

-

, (2008/06/13)

Compounds of general formula (I): STR1 in which: R1 and R2 each represent a hydrogen atom or, with the nitrogen and oxygen which bear them, form an --O--CO--N link, W represents a halogen atom or a lower alkyl or alkoxy group optionally substituted with one or more halogen atoms, such as trifluoromethyl, and m being between 0 and 3, A is a linear or branched alkyl radical comprising from 1 to 6 carbon atoms, R3 and R4 are defined in the description have medicinal properties.

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